EP1118458A1 - Polyacetalverbund und verfahren zu dessen herstellung - Google Patents

Polyacetalverbund und verfahren zu dessen herstellung Download PDF

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Publication number
EP1118458A1
EP1118458A1 EP00939119A EP00939119A EP1118458A1 EP 1118458 A1 EP1118458 A1 EP 1118458A1 EP 00939119 A EP00939119 A EP 00939119A EP 00939119 A EP00939119 A EP 00939119A EP 1118458 A1 EP1118458 A1 EP 1118458A1
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EP
European Patent Office
Prior art keywords
acid
polyacetal
acidic group
elastomer
polymer unit
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP00939119A
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English (en)
French (fr)
Other versions
EP1118458A4 (de
Inventor
Mitsuteru Mutsuda
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Daicel Evonik Ltd
Original Assignee
Daicel Degussa Co Ltd
Daicel Huels Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daicel Degussa Co Ltd, Daicel Huels Ltd filed Critical Daicel Degussa Co Ltd
Publication of EP1118458A1 publication Critical patent/EP1118458A1/de
Publication of EP1118458A4 publication Critical patent/EP1118458A4/de
Withdrawn legal-status Critical Current

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    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
    • B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B27/00—Layered products comprising a layer of synthetic resin
    • B32B27/28—Layered products comprising a layer of synthetic resin comprising synthetic resins not wholly covered by any one of the sub-groups B32B27/30 - B32B27/42
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L59/00—Compositions of polyacetals; Compositions of derivatives of polyacetals
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31507—Of polycarbonate
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31725—Of polyamide
    • Y10T428/31761—Next to aldehyde or ketone condensation product
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31786—Of polyester [e.g., alkyd, etc.]
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00—Stock material or miscellaneous articles
    • Y10T428/31504—Composite [nonstructural laminate]
    • Y10T428/31855—Of addition polymer from unsaturated monomers
    • Y10T428/31859—Next to an aldehyde or ketone condensation product

Definitions

  • the present invention relates to a composite member comprising a polyacetal resin and another polymeric material (specifically, an elastic material) directly adhering to each other, as well as to a production process thereof.
  • Polyacetal resins were launched into mass production by Du Pont (E.I.) de Nemours & Co. and Celanese Corp. in about the 1960s and have been used in a variety of fields since then, as they are very excellent in fatigue resistance and have satisfactory physical properties in balance such as friction/abrasion resistance, low-noise property, chemical resistance, creep resistance, and dimensional stability.
  • such a polyacetal resin has poor affinity to other organic materials due to its specific chemical structure, as compared with other engineering plastics, and therefore is used alone.
  • there is no appropriate adhesive to combine the polyacetal resin with another material as the polyacetal resin is resistant to adhesion.
  • there are strong demands to combine the polyacetal resin with an elastic material to make use of its satisfactory physical properties but the demands cannot be significantly responded to due to the above technical reasons.
  • an object of the present invention is to provide a composite which includes a polyacetal resin and another polymeric material firmly adhering to each other, and a production process thereof.
  • Another object of the present invention is to provide a composite which includes a polyacetal resin and another polymeric material directly adhering to each other without the medium of an adhesive.
  • the present inventors found that heating of a polyacetal resin and a thermoplastic resin or elastomer having an acidic group permits an interface between the both materials to firmly bind and fix with each other.
  • the present invention has been accomplished based on these findings.
  • the present invention provides, in an aspect, a polyacetal composite which includes a polymer unit (A) composed of a polyacetal resin, and a polymer unit (B) composed of a thermoplastic resin or elastomer having an acidic group, and the polymer unit (A) and the polymer unit (B) directly adhere to each other.
  • the acidic group includes, for example, a carboxyl group and a carboxylic anhydride group.
  • the thermoplastic resin or elastomer having an acidic group includes, for example, a copolymer having, as a comonomer, at least one selected from among acrylic acid, methacrylic acid, fumaric acid, maleic acid, maleic anhydride, and itaconic acid.
  • the thermoplastic resin or elastomer having an acidic group includes, for example, an acid-modified polystyrene and an acid-modified NBR (acid-modified nitrile rubber).
  • the present invention provides a process for producing a polyacetal composite which includes the step of bringing a composition containing a polyacetal resin into contact with a composition containing a thermoplastic resin or elastomer having an acidic group (including the case where the thermoplastic resin or elastomer having an acidic group alone is contained) under heating to thereby yield a composite including a polymer unit (A) composed of the polyacetal resin, and a polymer unit (B) composed of the thermoplastic resin or elastomer having an acidic group, in which the polymer unit (A) and the polymer unit (B) directly adhere to each other.
  • composition containing a polyacetal resin also includes the case where the composition contains a polyacetal resin alone.
  • composition containing a thermoplastic resin or elastomer having an acidic group also includes the case where the composition contains the thermoplastic resin or elastomer having an acidic group alone.
  • Fig. 1 is a schematic diagram illustrating a production process of a composite according to Example.
  • a polymer unit (A) is composed of a polyacetal resin.
  • the polyacetal resin polymers each having an acetal bond in a principle chain are acceptable, and polymers derived from formaldehyde which are generically referred to as polyoxymethylenes are specifically preferred.
  • Such polyacetal resins can be prepared by any production process, and there is not restraint in end group.
  • the polyoxymethylenes include, but are not limited to, ⁇ -polyoxymethylene, ⁇ -polyoxymethylene, ⁇ -polyoxymethylene, 8-polyoxymethylene, ⁇ -polyoxymethylene, Eu-polyoxymethylene, cyclic polyoxymethylene, and other polyoxymethylenes in which the overall principle chain is composed of oxymethylene structure, as well as those having another unit such as oxyethylene unit than oxymethylene in the principle chain.
  • Examples of the polyoxymethylenes in which the principle chain is composed of oxymethylene unit alone include “Delrin” of Du Pont (E.I.) de Nemours & Co. and “Tenac” of Asahi Chemical Industry Co., Ltd.
  • the polyoxymethylenes having another unit introduced into a principal chain include, for example, "Celcon” of Celanese Corp., “Duracon” of Polyplastics Co., Ltd., “Iupital” of Mitsubishi Gas Chemical Co., Ltd., "Ultraform” of BASF AG, and “Tenac C” of Asahi Chemical Industry Co., Ltd.
  • the polymer unit (A) may further comprise, in addition to the polyacetal resin, additional components that are generally incorporated intoplastics.
  • additional components include, but are not limited to, the other polymers, glass fibers and other fillers, oils and other various added substances, stabilizers, coloring agents, plasticizers, flame-retardants and other various additives.
  • a polymer unit (B) is composed of a thermoplastic resin or elastomer having an acidic group (e.g., an acid-modified polymer).
  • the acidic group may be contained in any moiety of a principle chain and side chain in the molecular structure of the thermoplastic resin or elastomer.
  • the thermoplastic resin or elastomer having an acidic group may be a single polymer, or a polymer alloy or polymer blend containing at least one polymer having an acidic group. In the latter, the polymer alloy or polymer blend may be composed of a polymer having an acidic group alone or may be a mixture of a polymer having an acidic group with a polymer having no acidic group.
  • Such acidic groups include, but are not limited to, carboxyl group and sulfonic group, as well as equivalents of these groups such as carboxylic anhydride group. Among them, carboxyl group and carboxylic anhydride group are specifically preferred as the acidic group.
  • thermoplastic resin is not specifically limited and includes, for example, styrenic resins having styrene as a principal monomer, acrylic resins having a (meth) acrylic ester as a principle monomer, olefinic resins having an olefin as a principle monomer, vinyl-chloride-based resins having vinyl chloride as a principle monomer, poly(vinyl alcohol)-based resins having vinyl alcohol as a principle monomer, fluororesins, polyamides, polycarbonates, poly(phenylene ether), poly(phenylene sulfide), polyarylates, polysulfones, poly(ether sulfone), and poly(ether ether ketone).
  • the elastomer includes so-called rubbers and thermoplastic elastomers.
  • rubbers include, but are not limited to, isoprene rubber (IR), butadiene rubber (BR), chloroprene rubber (CR), styrene-butadiene rubber (SBR), nitrile rubber (NBR), isobutylene-isoprene rubber (IIR), ethylene-propylene rubbers [ethylene-propylene copolymer (EPM), ternary ethylene-propylene rubber (EPDM)], acrylic rubbers (e.g., ACM and ANM), epichlorohydrin rubber, silicone rubber, fluororubber (FKM), urethane rubber (AU), and chlorosulfonated polyethylene (CSM).
  • the rubbers may be any of vulcanized rubbers and unvulcanized rubbers.
  • thermoplastic elastomers include, but are not limited to, styrene-butadiene-styrene block copolymers (SBS), hydrogenated SBS (SEBS), styrene-isoprene-styrene block copolymer (SIS), hydrogenated SIS (SEPS), and other styrene block copolymer-based thermoplastic elastomers; polyurethane-based thermoplastic elastomers; polyester-based thermoplastic elastomers; fluoropolymer-based thermoplastic elastomers; polyamide-based thermoplastic elastomers; and blends (TPO) of polypropylene with EPM or EPDM.
  • SBS styrene-butadiene-styrene block copolymers
  • SEBS hydrogenated SBS
  • SIS styrene-isoprene-styrene block copolymer
  • SEPS hydrogenated SIS
  • TPO blends
  • Techniques for introducing an acidic group into the thermoplastic resin or elastomer include, for example, a process in which a polymerizable unsaturated compound having an acidic group such as acrylic acid, methacrylic acid, fumaric acid, maleic acid, maleic anhydride, and itaconic acid is subjected as a comonomer to copolymerization with a major monomer component, and a process in which a monomer mixture containing a monomer having a reactive functional group is polymerized, and the resulting polymer is allowed to react with a compound having both a functional group which is reactive with the above reactive functional group, and an acidic group (e.g., the aforementioned acidic group).
  • an acidic group e.g., the aforementioned acidic group
  • the amount of the introduced acidic group can be appropriately selected within a range not adversely affecting characteristics which the thermoplastic resin or elastomer inherently possesses.
  • the proportion of the monomer having an acidic group is about 5 to 40% by mole relative to the total monomeric units.
  • thermoplastic resin or elastomer having an acidic group examples include acid-modified polystyrenes containing a carboxylic acid or carboxylic anhydride such as maleic anhydride (e.g., "Dylark D332" produced by Sekisui Chemical Co., Ltd.), and acid-modified NBR (e.g., "Nipol 1472” produced by Nippon Zeon Co., Ltd.).
  • acid-modified polystyrenes containing a carboxylic acid or carboxylic anhydride such as maleic anhydride (e.g., "Dylark D332" produced by Sekisui Chemical Co., Ltd.), and acid-modified NBR (e.g., "Nipol 1472" produced by Nippon Zeon Co., Ltd.).
  • the polymer unit (B) may further comprise a variety of additives, in addition to the thermoplastic resin or elastomer having an acidic group.
  • additives include, for example, vulcanizing agents, vulcanization accelerators, softeners, plasticizers, fillers, ageresistors, antioxidants, antiozonants, UV absorbents, tackifiers, lubricants, coloring agents, and flame-retardants.
  • the type and amount of these additives can be appropriately selected depending on required performances of the polymer unit (B).
  • thermoplastic resin or elastomer having an acidic group is a rubber
  • a vulcanizing agent, vulcanization accelerator, softener, plasticizer, and filler are added.
  • vulcanizing agents include conventional vulcanizing agents such as sulfur, sulfur-containing compounds, organic peroxides, and metal oxides.
  • the proportion of the vulcanizing agent is, for example, about 1 to 10 parts by weight relative to 100 parts by weight of the rubber.
  • the vulcanization accelerator can be appropriately selected depending on the type of the vulcanizing agent.
  • sulfur or a sulfur-containing compound for example, benzothiazoles, benzothiazolesulfenamides, dithiocarbamates, xanthogens, thioureas, dithiocarbamylsulfenamides, guanidines, and thiurams are used as the vulcanization accelerator.
  • 1,4-butanediol di(meth)acrylate, trimethylolpropane tri(meth)acrylate, and other (meth)acrylates, triallyl cyanurate, and other triallylates, and meta-phenylenedimaleimides are used as the vulcanization accelerator.
  • the proportion of the vulcanization accelerator can be selected depending on, for example, required physical properties of the rubber, vulcanization rate, and combination of the vulcanizing agent, and is, for example, about 0.5 to 5 parts by weight relative to 100 parts by weight of the rubber.
  • softener general petroleum process oils such as paraffin oils, naphthene oils, and aromatic oils are used, for example.
  • plasticizer for example, phthalic esters, sebacic esters, adipic esters, phosphoric esters, and other low molecular weight plasticizers, as well as various polyester-based plasticizers, and chlorinated polypropylenes can be used according to the application.
  • the amounts of the softener and plasticizer can be freely selected depending on the required physical properties of the rubber, for example, within a range from about 0 to about 150 parts by weight relative to 100 parts by weight of the rubber.
  • the fillers include, for example, those used in rubber compositions, such as carbon black, silicic acid, silicates, calcium carbonate, zinc oxide, barium sulfate, magnesium sulfate, talc, and kaolin.
  • the proportion of the filler can be selected within a range from about 10 to about 300 parts by weight relative to 100 parts by weight of the rubber, depending on required physical properties of the rubber.
  • the invented polyacetal composite can be produced by bringing, under heating, a composition containing a polyacetal resin into contact with a composition containing a thermoplastic resin or elastomer having an acidic group.
  • a heating temperature is higher than the glass transition temperature of the polyacetal resin constituting the polymer unit (A).
  • the heating temperature is higher than the glass transition temperature of the thermoplastic resin.
  • the heating temperature should be preferably selected within a range of vulcanization temperatures(e.g., about 110°C to 220°C).
  • the heating temperature of the composition containing the polyacetal resin and the composition containing the thermoplastic resin or elastomer having an acidic group is about 120°C to 200°C.
  • the heating and contact operation of the composition containing the polyacetal resin and the composition containing the thermoplastic resin or elastomer having an acidic group can be performed under a pressure.
  • the pressure in this case is, for example, about 50 to 2000 kgf/cm 2
  • a compression-bonding time is, for example, about 10 seconds to 60 minutes.
  • the invented polyacetal composite can be produced, for example, by (i) bringing a molded article, which is obtained by optionallymolding a composition containing the polyacetal resin, into contact with a composition containing the thermoplastic resin or elastomer having an acidic group (e.g., pellet-formorpowderedcomposition) under heating.
  • the molded article can be obtained by any conventional molding techniques such as hot press, injection molding, and extrusion molding.
  • the heating operation is generally performed in a mold meeting the shape of the target article, but the operation does not necessarily require a mold when the target shape is, for example, a sheet or film.
  • the rubber When a rubber is used as the thermoplastic resin or elastomer having an acidic group, the rubber may be a vulcanized rubber or unvulcanized rubber. Especially, when an unvulcanized rubber is used, an appropriate pressure should be preferably applied to efficiently degas volatile components or gaseous components in the unvulcanized rubber. Specifically, hot press or injection molding, for example, is used in the heating step. In this connection, when an unvulcanized rubber is used, a satisfactory composite can be obtained by vulcanizing the rubber in this step.
  • the invented polyacetal composite can also be obtained by (ii) bringing a molded article, which is obtained from a composition containing the thermoplastic resin or elastomer having an acidic group by a conventional molding technique, into contact with a composition containing the polyacetal resin (e.g., pellet-form or powdered composition) for example in a mold under heating (and where necessary under a pressure). Also in this case, hot press or injection molding or another technique is employed.
  • a molded article which is obtained from a composition containing the thermoplastic resin or elastomer having an acidic group by a conventional molding technique
  • a composition containing the polyacetal resin e.g., pellet-form or powdered composition
  • hot press or injection molding or another technique is employed.
  • the invented polyacetal composite can be obtained by (iii) melting one composition of the composition containing the polyacetal resin and the composition containing the thermoplastic resin or elastomer having an acidic group, and adding a molded article of the other composition to the melted composition, kneading the mixture, and cooling the kneaded product.
  • the shape of the molded article added to the melted composition is not specifically limited.
  • the invented polyacetal composite can be used in a wide range of applications such as gears, rollers, seismic isolators, vibration insulators, and sliding members.
  • the present invention can combine a polyacetal resin with another polymeric material, specifically with an elastic material, and the resulting composite has a very high adhesion strength in its composite interface. Additionally, the polyacetal resin is directly bonded to the other polymeric material and the use of an adhesive or a special treatment is not required, to thereby simplify the steps to a great extent. Furthermore, the production does not require the use of a harmful solvent.
  • thermoplastic resin or elastomer B (B1 to B8) (about 6.5 cm 3 in case of B1 to B3, B5, and B7) was placed in such a manner that an end of the thermoplastic resin or elastomer B was in contact with the other end of the molded article of A in the length direction.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Laminated Bodies (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)
EP00939119A 1999-06-24 2000-06-22 Polyacetalverbund und verfahren zu dessen herstellung Withdrawn EP1118458A4 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP17768199 1999-06-24
JP17768199A JP4053186B2 (ja) 1999-06-24 1999-06-24 ポリアセタール複合体及びその製造法
PCT/JP2000/004079 WO2000078542A1 (fr) 1999-06-24 2000-06-22 Composite au polyacetal et procede de production

Publications (2)

Publication Number Publication Date
EP1118458A1 true EP1118458A1 (de) 2001-07-25
EP1118458A4 EP1118458A4 (de) 2002-01-23

Family

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Family Applications (1)

Application Number Title Priority Date Filing Date
EP00939119A Withdrawn EP1118458A4 (de) 1999-06-24 2000-06-22 Polyacetalverbund und verfahren zu dessen herstellung

Country Status (6)

Country Link
US (1) US6517949B1 (de)
EP (1) EP1118458A4 (de)
JP (1) JP4053186B2 (de)
KR (1) KR20010072884A (de)
CN (1) CN1128714C (de)
WO (1) WO2000078542A1 (de)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1273433A1 (de) * 2001-01-15 2003-01-08 Daicel-Degussa Ltd. Verbundmaterial und methode zu dessen herstellung
WO2005065913A1 (de) * 2003-12-24 2005-07-21 Ticona Gmbh Verbundkörper, verfahren zu dessen herstellung und dessen verwendung
US7858202B2 (en) 2004-09-29 2010-12-28 Ticona Gmbh Composite bodies having a polyacetal portion and a thermoplastic vulcanized elastomer portion, processes for making the same, articles including such bodies and uses therefor

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DE19845235C2 (de) * 1998-10-02 2002-05-16 Ticona Gmbh Verbundkörper aus Polyacetal und Styrol-Olefin-Elastomeren und Verfahren zu dessen Herstellung
DE10104565A1 (de) * 2000-02-02 2001-10-31 Asahi Chemical Ind Integrierte Strukturteile aus thermoplastischen Harzen
EP1225036B1 (de) * 2001-01-17 2004-10-27 Ponachem AG Verbundkörper
US7147905B2 (en) * 2001-10-19 2006-12-12 Kuraray Co., Ltd. Layered product and medical supply comprising the layered product
DE10361190A1 (de) * 2003-12-24 2005-07-28 Ticona Gmbh Verbundkörper, Verfahren zu dessen Herstellung und dessen Verwendung
US9770856B2 (en) * 2008-05-29 2017-09-26 National University Corporation Kyoto Insitute Of Technology Composite molded article having two-layer structure
JP6256671B1 (ja) * 2016-09-09 2018-01-10 Nok株式会社 ポリアセタール樹脂−ニトリルゴム複合体
CN108290397B (zh) * 2016-09-09 2019-07-16 Nok株式会社 聚缩醛树脂-丁腈橡胶复合体
CN110054861B (zh) * 2019-04-11 2021-06-18 金发科技股份有限公司 一种聚甲醛复合材料及其制备方法和sebs在聚甲醛中作为消光剂的用途

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1273433A1 (de) * 2001-01-15 2003-01-08 Daicel-Degussa Ltd. Verbundmaterial und methode zu dessen herstellung
EP1273433A4 (de) * 2001-01-15 2003-04-16 Daicel Degussa Ltd Verbundmaterial und methode zu dessen herstellung
WO2005065913A1 (de) * 2003-12-24 2005-07-21 Ticona Gmbh Verbundkörper, verfahren zu dessen herstellung und dessen verwendung
US7858202B2 (en) 2004-09-29 2010-12-28 Ticona Gmbh Composite bodies having a polyacetal portion and a thermoplastic vulcanized elastomer portion, processes for making the same, articles including such bodies and uses therefor

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KR20010072884A (ko) 2001-07-31
JP2001001451A (ja) 2001-01-09
EP1118458A4 (de) 2002-01-23
CN1314843A (zh) 2001-09-26
US6517949B1 (en) 2003-02-11
CN1128714C (zh) 2003-11-26
JP4053186B2 (ja) 2008-02-27
WO2000078542A1 (fr) 2000-12-28

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